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International Heart Journal|November 16, 2020
Age-Dependent Echocardiographic and Pathologic Findings in a Rat Model with Duchenne Muscular Dystrophy Generated by CRISPR/Cas9 Genome EditingHidetoshi Sugihara, Koichi Kimura, Keitaro Yamanouchi, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 17, 2019
Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD GeneYusuke Echigoya, Kenji Rowel Q Lim, Dyanna Melo, et al.Scientific Reports|March 17, 2023
Full-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse modelYosuke Hiramuki, Satoshi Abe, Narumi Uno, et al.BMC Medicine|November 19, 2020
The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx miceYasunari Matsuzaka, Jun Tanihata, Yoshiko Ooshima, et al.Nature Communications|September 26, 2024
Heteroduplex oligonucleotide technology boosts oligonucleotide splice switching activity of morpholino oligomers in a Duchenne muscular dystrophy mouse modelJuri Hasegawa, Tetsuya Nagata, Kensuke Ihara, et al.Molecular & Cellular Proteomics : MCP|September 30, 2020
Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular DystrophyTirsa L E van Westering, Henrik J Johansson, Britt Hanson, et al.Journal of Cachexia, Sarcopenia and Muscle|April 4, 2022
Involvement of Parkin-mediated mitophagy in the pathogenesis of chronic obstructive pulmonary disease-related sarcopeniaAkihiko Ito, Mitsuo Hashimoto, Jun Tanihata, et al.Scientific Reports|April 29, 2021
Transcriptome analysis of gravitational effects on mouse skeletal muscles under microgravity and artificial 1 g onboard environmentRisa Okada, Shin-Ichiro Fujita, Riku Suzuki, et al.Pageof 4